Kartagener syndrome

disorder

SNOMED 42402006CUI C0022521

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Absent outer dynein arms

Always present (100%)HP:0012256

Bronchitis, recurrent

Always present (100%)HP:0002837

Chronic ear infection

Always present (100%)HP:0000389

Chronic sinus disease

Always present (100%)HP:0011109

Immotile cilia

Always present (100%)HP:0012263

Pulmonary atelectasis

Always present (100%)HP:0100750

Abnormality of the cornea

HP:0000481

Absent spleen

HP:0001746

Aplasia of frontal sinus

HP:0002688

Bronchiectasis

HP:0002110

Chronic rhinitis

HP:0002257

Communicating hydrocephalus

HP:0001334

Headache

HP:0002315

Hearing loss, conductive

HP:0000405

Lack of coordinated beating of respiratory cilia

HP:0012265

Lost smell

HP:0000458

Male infertility

HP:0003251

Nasal polyps

HP:0100582

Pneumonia

HP:0002090

Situs inversus totalis

HP:0001696

Related Conditions

Immotile cilia syndrome(parent)

Dextrocardia(parent)

Chronic sinusitis(parent)

Bronchiectasis(parent)

Chronic heart disorder(parent)

Cardiovascular system hereditary disorder(parent)

Quick Facts

SNOMED CT: 42402006
UMLS CUI: C0022521
Fully Specified Name: Kartagener syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 20

Medical Disclaimer

This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.

Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.